Liberty Pharma
Accelerate Development, Ensure Compliance, Maximize Market Access
Handles regulatory submissions end-to-end across FDA, EMA, DCGI, ANVISA, COFEPRIS.
Achieves 8 months faster time-to-market with 70-90% time savings.
Modular deployment from single workflows to complete automation.
Key Capabilities:
- Regulatory automation
- Clinical trial optimization
- Supply chain & API management
- Quality assurance
- Pharmacovigilance